Variant #0000656605 (NC_000010.10:g.95422918A>G, NM_006204.3:c.2501A>G (PDE6C))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.95422918A>G
DNA change (hg38) g.93663161A>G
Published as PDE6C(NM_006204.3):c.2501A>G (p.E834G), PDE6C(NM_006204.4):c.2501A>G (p.E834G)
ISCN -
DB-ID PDE6C_000031 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00232 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE6C NM_006204.3 ?/. - c.2501A>G r.(?) p.(Glu834Gly)
FRA10AC1 NM_145246.4 ?/. - c.*6665T>C r.(=) p.(=)


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